EVALUATION OF A SINGLE DILUTION ELISA SYSTEM FOR DETECTION OF SEROCONVERSION TO BOVINE VIRAL DIARRHEA VIRUS, BOVINE RESPIRATORY SYNCYTIAL VIRUS, PARAINFLUENZA-3 VIRUS, AND INFECTIOUS BOVINE-RHINOTRACHEITIS VIRUS - COMPARISON WITH TESTING BY VIRUS NEUTRALIZATION AND HEMAGGLUTINATION INHIBITION
Da. Graham et al., EVALUATION OF A SINGLE DILUTION ELISA SYSTEM FOR DETECTION OF SEROCONVERSION TO BOVINE VIRAL DIARRHEA VIRUS, BOVINE RESPIRATORY SYNCYTIAL VIRUS, PARAINFLUENZA-3 VIRUS, AND INFECTIOUS BOVINE-RHINOTRACHEITIS VIRUS - COMPARISON WITH TESTING BY VIRUS NEUTRALIZATION AND HEMAGGLUTINATION INHIBITION, Journal of veterinary diagnostic investigation, 10(1), 1998, pp. 43-48
A single-dilution quantitative enzyme-linked immunosorbent assay (ELIS
A) system, based on commercial ELISA kits, for the simultaneous detect
ion of seroconversion to bovine viral diarrhea virus (BVDV), bovine re
spiratory syncytial virus (BRSV), parainfluenza-3 virus (PI3V), and in
fectious bovine rhinotracheitis virus (IBRV) was evaluated by testing
acute and convalescent serum pairs from 564 cattle in 145 outbreaks of
respiratory disease. Seroconversion to BVDV, BRSV, PI3V and IBRV was
detected in 8.0%, 19.0%, 13.7%, and 7.4%, respectively, of serum pairs
tested. Seroconversion was detected in 60.7% of herds and 34.6% of an
imals tested. Infection with 2 or more viruses was found in 46.6% of t
hese herds and in 27.2% of these animals. The majority of BVDV infecti
ons (62%) were associated with other virus infections, suggesting that
BVDV may potentiate infection with other agents rather than being a p
rimary pathogen of the respiratory tract. The results were compared wi
th those obtained by virus neutralization and hemagglutination inhibit
ion testing, and the sensitivity, specificity, and overall correlation
were calculated. Sensitivities of 92%, 95%, 100%, and 100% were obtai
ned for BVDV, BRSV, PI3V, and IBRV, respectively. The corresponding sp
ecificity values were 89%, 92%, 86%, and 91%. The overall correlation
for each virus was 90%, 93%, 90%, and 93%, respectively. These results
demonstrate that this ELISA system may be used successfully to detect
seroconversion in serum pairs, highlight the frequency of multiple vi
ral infections in outbreaks of respiratory disease, and provide furthe
r evidence of an immunosuppressive role for BVDV infections.